235 related articles for article (PubMed ID: 15333589)
1. An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability.
Demuth I; Frappart PO; Hildebrand G; Melchers A; Lobitz S; Stöckl L; Varon R; Herceg Z; Sperling K; Wang ZQ; Digweed M
Hum Mol Genet; 2004 Oct; 13(20):2385-97. PubMed ID: 15333589
[TBL] [Abstract][Full Text] [Related]
2. Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein.
Krüger L; Demuth I; Neitzel H; Varon R; Sperling K; Chrzanowska KH; Seemanova E; Digweed M
Carcinogenesis; 2007 Jan; 28(1):107-11. PubMed ID: 16840438
[TBL] [Abstract][Full Text] [Related]
3. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks.
Digweed M; Sperling K
DNA Repair (Amst); 2004; 3(8-9):1207-17. PubMed ID: 15279809
[TBL] [Abstract][Full Text] [Related]
4. Clinical variability and expression of the NBN c.657del5 allele in Nijmegen Breakage Syndrome.
Lins S; Kim R; Krüger L; Chrzanowska KH; Seemanova E; Digweed M
Gene; 2009 Nov; 447(1):12-7. PubMed ID: 19635536
[TBL] [Abstract][Full Text] [Related]
5. Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis.
Dumon-Jones V; Frappart PO; Tong WM; Sajithlal G; Hulla W; Schmid G; Herceg Z; Digweed M; Wang ZQ
Cancer Res; 2003 Nov; 63(21):7263-9. PubMed ID: 14612522
[TBL] [Abstract][Full Text] [Related]
6. MRI evidence of white matter damage in a mouse model of Nijmegen breakage syndrome.
Assaf Y; Galron R; Shapira I; Nitzan A; Blumenfeld-Katzir T; Solomon AS; Holdengreber V; Wang ZQ; Shiloh Y; Barzilai A
Exp Neurol; 2008 Jan; 209(1):181-91. PubMed ID: 17976584
[TBL] [Abstract][Full Text] [Related]
7. Nibrin functions in Ig class-switch recombination.
Kracker S; Bergmann Y; Demuth I; Frappart PO; Hildebrand G; Christine R; Wang ZQ; Sperling K; Digweed M; Radbruch A
Proc Natl Acad Sci U S A; 2005 Feb; 102(5):1584-9. PubMed ID: 15668383
[TBL] [Abstract][Full Text] [Related]
8. Expression of full-length NBS1 protein restores normal radiation responses in cells from Nijmegen breakage syndrome patients.
Ito A; Tauchi H; Kobayashi J; Morishima K; Nakamura A; Hirokawa Y; Matsuura S; Ito K; Komatsu K
Biochem Biophys Res Commun; 1999 Nov; 265(3):716-21. PubMed ID: 10600486
[TBL] [Abstract][Full Text] [Related]
9. Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.
Seeman P; Gebertová K; Paderová K; Sperling K; Seemanová E
Pediatr Neurol; 2004 Mar; 30(3):195-200. PubMed ID: 15033202
[TBL] [Abstract][Full Text] [Related]
10. Mild Nijmegen breakage syndrome phenotype due to alternative splicing.
Varon R; Dutrannoy V; Weikert G; Tanzarella C; Antoccia A; Stöckl L; Spadoni E; Krüger LA; di Masi A; Sperling K; Digweed M; Maraschio P
Hum Mol Genet; 2006 Mar; 15(5):679-89. PubMed ID: 16415040
[TBL] [Abstract][Full Text] [Related]
11. The role of NBS1 in DNA double strand break repair, telomere stability, and cell cycle checkpoint control.
Zhang Y; Zhou J; Lim CU
Cell Res; 2006 Jan; 16(1):45-54. PubMed ID: 16467875
[TBL] [Abstract][Full Text] [Related]
12. New mutations and protein variants of NBS1 are identified in cancer cell lines.
Tessitore A; Biordi L; Flati V; Toniato E; Marchetti P; Ricevuto E; Ficorella C; Scotto L; Giannini G; Frati L; Masciocchi C; Tombolini V; Gulino A; Martinotti S
Genes Chromosomes Cancer; 2003 Feb; 36(2):198-204. PubMed ID: 12508248
[TBL] [Abstract][Full Text] [Related]
13. Cancer risk of heterozygotes with the NBN founder mutation.
Seemanová E; Jarolim P; Seeman P; Varon R; Digweed M; Swift M; Sperling K
J Natl Cancer Inst; 2007 Dec; 99(24):1875-80. PubMed ID: 18073374
[TBL] [Abstract][Full Text] [Related]
14. Nijmegen breakage syndrome: consequences of defective DNA double strand break repair.
Digweed M; Reis A; Sperling K
Bioessays; 1999 Aug; 21(8):649-56. PubMed ID: 10440861
[TBL] [Abstract][Full Text] [Related]
15. Inactivation of the Nijmegen breakage syndrome gene leads to excess centrosome duplication via the ATR/BRCA1 pathway.
Shimada M; Sagae R; Kobayashi J; Habu T; Komatsu K
Cancer Res; 2009 Mar; 69(5):1768-75. PubMed ID: 19244116
[TBL] [Abstract][Full Text] [Related]
16. [Genes and cancer. NBS1 (Nijmegen breakage syndrome). Repair gene].
Soussi T
Bull Cancer; 1999 Oct; 86(10):803-4. PubMed ID: 10610129
[No Abstract] [Full Text] [Related]
17. Mutational inactivation of the nijmegen breakage syndrome gene (NBS1) in glioblastomas is associated with multiple TP53 mutations.
Watanabe T; Nobusawa S; Lu S; Huang J; Mittelbronn M; Ohgaki H
J Neuropathol Exp Neurol; 2009 Feb; 68(2):210-5. PubMed ID: 19151620
[TBL] [Abstract][Full Text] [Related]
18. Extreme variation in apoptosis capacity amongst lymphoid cells of Nijmegen breakage syndrome patients.
Thierfelder N; Demuth I; Burghardt N; Schmelz K; Sperling K; Chrzanowska KH; Seemanova E; Digweed M
Eur J Cell Biol; 2008 Feb; 87(2):111-21. PubMed ID: 17977616
[TBL] [Abstract][Full Text] [Related]
19. Conditional inactivation of the NBS1 gene in the mouse central nervous system leads to neurodegeneration and disorganization of the visual system.
Baranes K; Raz-Prag D; Nitzan A; Galron R; Ashery-Padan R; Rotenstreich Y; Assaf Y; Shiloh Y; Wang ZQ; Barzilai A; Solomon AS
Exp Neurol; 2009 Jul; 218(1):24-32. PubMed ID: 19345213
[TBL] [Abstract][Full Text] [Related]
20. A novel function of DNA repair molecule Nbs1 in terminal differentiation of the lens fibre cells and cataractogenesis.
Yang YG; Frappart PO; Frappart L; Wang ZQ; Tong WM
DNA Repair (Amst); 2006 Aug; 5(8):885-93. PubMed ID: 16790366
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
